US20100330085A1 - Method of treatment, prophylaxis and diagnosis of pathologies of the bone - Google Patents

Method of treatment, prophylaxis and diagnosis of pathologies of the bone Download PDF

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US20100330085A1
US20100330085A1 US12/841,697 US84169710A US2010330085A1 US 20100330085 A1 US20100330085 A1 US 20100330085A1 US 84169710 A US84169710 A US 84169710A US 2010330085 A1 US2010330085 A1 US 2010330085A1
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gene
bone
expression
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protein
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Anna Kathleen Coussens
Angela Mary Van Daal
Barry Crampton Powell
Peter John Anderson
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Womens and Childrens Health Research Institute
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/106—Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/158—Expression markers

Definitions

  • the present invention relates generally to the fields of treatment, prophylaxis and diagnosis. More particularly, the present invention identifies genes and gene products associated with bone morphogenesis and pathologies of the bone. Even more particularly, the present invention contemplates the regulation of expression of these genes or the activity of the gene products in the treatment, prophylaxis and diagnosis of bone pathologies. Cell-based therapies and manipulation of cells in in vitro culture also form part of the present invention.
  • Bone pathologies including bone cancers, fractures, craniosynostosis, osteoporosis and other biochemical or structural deficiencies can cause severe impairment, loss of quality of life and premature death to affected subjects.
  • Surgical or other physical intervention has been the major method of dealing with many of these pathologies.
  • the human skull is comprised of 45 bony elements, separated by fibrous joints known as sutures (Wilkie and Morriss-Kay, Nat Rev Genet. 2(6):458-468, 2001).
  • the bones which surround the brain are called calvaria and develop through intramembranous ossification. This is in contrast to the bones which comprise the cranial base and facial region, which form by the more common method of endochondral ossification.
  • the calvarial sutures need to remain as fibrous joints (unfused) until the brain has stopped growing and the rest of the skull, particularly the facial region, stops growing to allow for the movement of bones in relation to the new growth.
  • Calvarial bones first form from the condensation of ectomesenchyme (primary center of ossification) and then differentiation into osteoprogenitors, preosteoblasts and finally osteoblasts which secrete a collagen-proteoglycan extracellular matrix (ECM). Mineralization of the ECM traps osteoblasts which differentiate into osteocytes. The signals that initiate the bone formation are unclear.
  • ECM collagen-proteoglycan extracellular matrix
  • craniosynostosis Premature fusion of calvarial sutures, known as craniosynostosis, occurs in 1 in 2500 live births in the Western World (Wilkie, Am J Med Genet. 90(1):82-84, 2000) and is the second most common cranial defect. Fusion can be due to either premature bony bridging between apposed bones, or increased bone growth resulting in extremely overlapped bones. It can occur at only one or multiple calvarial sutures, it may occur before or after birth and it may be sporadic or syndromic. The study of craniosynostosis is important because it provides a model to study the causes of suture fusion bone growth and differentiation and, therefore, the factors regulating sutural maintenance and fusion. The known causes of craniosynostosis are varied, including monogenic conditions due to gene mutations, metabolic disorders, haematologic disorders and teratogens.
  • Invasive surgery is required to correct the facial abnormalities caused by craniosynostosis, by re-opening the fused section of tissue.
  • removal of the fused tissue allows the skull to regrow normally and bone is replaced within a short period of time.
  • multiple surgeries are required to continually re-open the tissues as the bones re-fuse too early.
  • the identification of therapeutic agents which would limit the premature re-fusion of the sutures, or which can be used to stop premature fusion of the sutures, especially when the presence of a genetic abnormality is first detected, would be highly desirable.
  • the culturing of suture mesenchyme is a common method to study the process of suture mesenchyme differentiation in vitro. There is a need, therefore, to identify biomarkers which assist in determining the stage of differentiation of osteoblasts.
  • the ECM of calvarial sutures consists of 90% type 1 collagens ( ⁇ 1(I) coll and ⁇ 2(I) coll), cell adhesion proteins (osteopontin (OP), fibronectin and thrombospondin), calcium-binding proteins (osteonectin (ON), and bone sialoprotein (BSP)), proteins involved in mineralization (osteocalcin (OC)) and enzymes (collagenase and alkaline phosphatase (ALP)) [Ducy et al, Cell 89(5):747-754, 1997; Robbins, Robbins Pathologic Basis of Disease, 1999].
  • Collagen is the earliest factor expressed in osteoprogenitor cells, followed by ALP, ON, BSP and finally OC in post-proliferative osteoblasts.
  • OP is expressed virtually in all proliferating osteoprogenitor and preosteoblast cells, while low BSP expression has also been identified before collagen expression in progenitor cells (Liu et al, J Cell Sci 116(9):1787-1796, 2003).
  • the current markers of osteoblast phenotype are, therefore, Col1, ALP, BSP, ON and OC. Research shows, however, that these markers have a large overlap of expression and do not uniquely identify the cells from each stage of differentiation (Liu et al, 2003 supra).
  • differentially expressed genes associated with bone pathologies have been identified.
  • the identification of these genes enables the development of therapeutic, prophylactic, diagnostic and tissue culture protocols in the treatment, prophylaxis and management of a range of bone pathologies including bone cancer, bone resorption and repair, bone fracture, suture-based cranial abnormalities including craniosynostosis, cytoskeletal disorders, osteoporosis, mineralization deficiencies and other biochemical or structural deficiencies.
  • the present invention further enables the promotion of bone health including bone growth.
  • the genes may also be considered as biomarkers for bone pathologies and hence may be useful in the diagnosis of a range of disorders or risk of development of same or a state of bone health.
  • Manipulation of gene expression or the activity of the gene product is also useful in in vitro cell culture protocols such as in the development of adipose-derived stromal cells, bone marrow-derived stromal cells, osteoclasts and osteoblasts.
  • the genes identified relate generally to bone cell proliferation (as typified by unfused sutures) and bone cell differentiation (as typified by fusing sutures).
  • one aspect of the present invention contemplates a method for the treatment or prophylaxis of a bone pathology including reducing the risk of developing a bone pathology in a subject, said method comprising administering to said subject an effective amount of an agent which modulates expression of genetic material or the activity of encoded products of the genetic material wherein the genetic material is differentially expressed in unfused versus fused calvarial sutures.
  • the present invention further provides the use of a set of biomarkers comprising one or more genes or gene products differentially expressed in unfused sutures compared to fused calvarial sutures in a subject in the manufacture of a medicament or development of a diagnostic protocol for a bone pathology.
  • the preferred subject is a human.
  • Reference to a “biomarker” includes a gene or gene product.
  • a “gene product” includes a protein or RNA.
  • FIG. 1 is a graphical representation of expression levels of the top 8 differentially regulated genes between fused and unfused sutures.
  • FIGS. 2( a ) and ( c ) and FIG. 2( b ) are graphical and photographic representations, respectively, which show mRNA and protein validation of differential expression identified by microarray analysis.
  • (a) Real-time QRT-PCR analysis of six genes with increased expression in unfused sutures (C1QTNF3 short isoform, RBP4, GPC3, PTN, PRELP, FMOD) and three genes with increased expression in fused sutures (ANXA3, WIF1 and CYFIP2) for unfused, fusing and fused suture tissue isolated from sagittal, coronal, lambdoid and metopic sutures.
  • FIGS. 3( a ) through ( c ) are photographic representations showing the expression pattern of two of the preferred genes in sutures.
  • (c-d) Serial immunofluorescence (c) and H&E sections (d) showing RBP4 located in cells in the region between calcified tissue (bn) and mesenchyme (m) (unfused left lambdoid suture).
  • RBP4 was localized to the cytoplasm of osteoblasts (ob) lining the developing bone, those being trapped in the osteoid (arrow head), and osteocytes (unfused coronal suture).
  • the present invention provides differentially expressed genes in the form of biomarkers which define targets for therapeutic, prophylactic and diagnostic protocols for bone pathologies in a subject.
  • the biomarkers comprise a set of genes or gene products differentially expressed in unfused sutures compared to fused sutures.
  • the unfused sutures versus fused sutures are in a subject with a suture-based cranial abnormality, such as, but not limited to, craniosynostosis.
  • biomarkers enable therapeutic, prophylactic and diagnostic protocols to be developed for a range of bone pathologies including bone cancers, bone resorption and repair, fracture management, suture-based cranial abnormalities such as craniosynostosis, cytoskeletal disorders, osteoporosis, and mineralization deficiencies or other biochemical or structural deficiencies.
  • the biomarkers are also useful in promoting bone growth or maintaining a state of bone health.
  • the biomarkers are referred to herein as a “target gene” or “target protein” or “target gene expression product”.
  • a gene includes a single gene, as well as two or more genes; reference to “an agent” includes reference to a single agent or two or more agents; reference to “the bone pathology” includes one bone pathology or multiple bone pathologies; and so on.
  • bone pathology includes any disorder or deficiency in the bone including but not limited to conditions of bone cancer, deficient bone mineralization or where bone repair is required such as following a fracture, green stick or bone chip, suture-based cranial disorders such as craniosynostosis, cytoskeletal disorders, osteoporosis or other biochemical or structural deficiencies.
  • the term “bone pathology” is not to be considered limiting to any one condition, disease or deficiency. One particular condition, however, is craniosynostosis.
  • the term “bone pathology” also refers to a level of bone health. Hence, certain target genes or gene products may be useful in maintaining or promoting bone health.
  • a wide variety of conditions that result in loss of bone mineral content, for example, is contemplated by the present invention.
  • Subjects with such conditions may be identified through clinical diagnosis utilizing well known techniques.
  • Representative examples of diseases that may be treated included dysplasias, wherein there is abnormal growth or development of bone such as in achondroplasia, cleidocranial dysostosis, enchondromatosis, fibrous dysplasia, Gaucher's disease, hypophosphatemic rickets, Marfan's syndrome, multiple hereditary exostoses, neurofibromatosis, osteogenesis imperfecta, oesteopetrosis, osteopoikilosis, sclerotic lesions, fractures, periodontal disease, pseudoarthrosis and pyogenic osteomyelitis.
  • Another condition contemplated herein includes bone cancer wherein there is abnormal growth of bone cells in bone or other tissue to which bone cells have metastasized.
  • Other conditions contemplated herein include a wide variety of causes of osteopenia (i.e. a condition that causes greater than one standard deviation of bone mineral content or density below peak skeletal mineral content at youth).
  • causes of osteopenia i.e. a condition that causes greater than one standard deviation of bone mineral content or density below peak skeletal mineral content at youth.
  • Representative examples of such conditions include those conditions caused by anemia, steroids, heparin, scurvy, malnutrition, calcium deficiency, idiopathic osteoporosis, congenital osteopenia or osteoporosis, transient regional osteoporosis and osteomalacia.
  • craniosynostosis refers to the premature fusion of calvarial sutures.
  • the condition may arise from any number of conditions including Apert, Beare-Stevenson, Boston, Crouzon, Jackson-Weiss, Pfeiffer, Saethre-Chotzen and Muenke syndrome. Over 100 syndromes can cause craniosynostosis (see Muenke and Wilkie, 2000 supra).
  • pathology does not necessarily mean the treatment of a disease condition.
  • Situations where the subject biomarkers may be useful for non-disease conditions is in the elderly, young infants, athletes and non-human animals such as horses.
  • bone growth may be promoted in subjects where it is sub-optimal; bone growth may be inhibited in subjects with excessive bone growth; and bone cancer growth can be inhibited.
  • compound used interchangeably herein to refer to a chemical compound that induces a desired pharmacological and/or physiological effect.
  • the terms also encompass pharmaceutically acceptable and pharmacologically active ingredients of those active agents specifically mentioned herein including but not limited to salts, esters, amides, prodrugs, active metabolites, analogs and the like.
  • a compound When the terms “compound”, “agent”, “chemical agent” “pharmacologically active agent”, “medicament”, “active” and “drug” are used, then it is to be understood that this includes the active agent per se as well as pharmaceutically acceptable, pharmacologically active salts, esters, amides, prodrugs, metabolites, analogs, etc.
  • the aforementioned compounds may specifically modulate expression of one or more differentially expressed genes (i.e. up-regulate or down-regulate expression as the case maybe) or they may modulate the activity of a gene product (i.e. increase or decrease the activity of a gene product) or they may replace an ineffective or low level of a gene product.
  • the compounds contemplated herein may be useful in genetic therapy or in protein replacement or protein inhibitory therapy.
  • the compound may be DNA, RNA, an antisense molecule, a sense molecule, double stranded or single stranded RNA or DNA, short interfering RNA (siRNA), RNA interference (RNAi) or a complex of a nucleic acid and a ribonuclease.
  • siRNA short interfering RNA
  • RNAi RNA interference
  • complex of a nucleic acid and a ribonuclease a complex of a nucleic acid and a ribonuclease.
  • references to a “compound”, “agent”, “chemical agent” “pharmacologically active agent”, “medicament”, “active” and “drug” includes combinations of two or more active agents.
  • a “combination” also includes multi-part such as a two-part composition where the agents are provided separately and given or dispensed separately or admixed together prior to dispensation.
  • a multi-part pharmaceutical pack may have two or more agents separately maintained.
  • an agent as used herein mean a sufficient amount of the agent to provide the desired therapeutic or physiological effect or outcome.
  • Such an effect or outcome includes modulating the expression or activity of a target gene or gene product or in the physiological outcome of intervention (such as amelioration of symptoms).
  • Undesirable effects e.g., side-effects, are sometimes manifested along with the desired therapeutic effect; hence, a practitioner balances the potential benefits against the potential risks in determining what is an appropriate “effective amount”.
  • the exact amount required will vary from subject to subject, depending on the species, age and general condition of the subject, mode of administration and the like. Thus, it may not be possible to specify an exact “effective amount”. However, an appropriate “effective amount” in any individual case may be determined by one of ordinary skill in the art using only routine experimentation.
  • the “effective amount” also includes an amount to promote bone growth or overall health.
  • excipient or diluent a pharmaceutical vehicle comprised of a material that is not biologically or otherwise undesirable, i.e. the material may be administered to a subject along with the selected active agent without causing any or a substantial adverse reaction.
  • Carriers may include excipients and other additives such as diluents, detergents, coloring agents, wetting or emulsifying agents, pH buffering agents, preservatives and the like.
  • a “pharmacologically acceptable” salt, ester, emide, prodrug or derivative of a compound as provided herein is a salt, ester, amide, prodrug or derivative that this not biologically or otherwise undesirable.
  • Treating” a subject may involve prevention of a condition or other adverse physiological event in a susceptible individual as well as treatment of a clinically symptomatic individual by ameliorating the symptoms of the condition.
  • the term “prophylaxis” may also be used.
  • a “subject” as used herein refers to an animal, preferably a mammal and more preferably human who can benefit from the pharmaceutical formulations and methods of the present invention. There is no limitation on the type of animal that could benefit from the presently described pharmaceutical formulations and methods. A subject regardless of whether a human or non-human animal may be referred to as an individual, patient, animal, host or recipient.
  • the compounds and methods of the present invention have applications in human medicine, veterinary medicine as well as in general, domestic or wild animal husbandry.
  • polypeptide “peptide” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues.
  • the terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical analog of a corresponding naturally occurring amino acid, naturally occurring amino acid polymers or recombinant polymers.
  • target gene or “target gene product” or “target protein” includes a gene or its expression product which is up-regulated or down-regulated in unfused versus fused sutures.
  • a list of genes is provided in Tables 2, 3 and 4 which are encompassed by the term “target genes”.
  • the expression products of these genes are examples of “target gene products”.
  • antibody includes various forms of modified or altered antibodies, such as an intact immunoglobulin, an Fv fragment containing only the light and heavy chain variable regions, an Fv fragment linked by a disulfide bond (Brinkmann et al, Proc. Natl, Acad. Sci. USA, 90:547-551, 1993), an Fab or (Fab)′2 fragment containing the variable regions and parts of the constant regions, a single-chain antibody and the like (Bird et al, Science 242:424-426, 1988; Huston et al, Proc. Nat. Acad. Sci. USA, 85:5879-5883, 1988).
  • the antibody may be of animal (especially mouse, rat, sheep or goat) or human origin or may be chimeric (Morrison et al, Proc. Nat. Acad. Sci. USA, 81:6851-6855, 1984) or humanized (Jones et al, Nature 321:522-525, 1986).
  • nucleic acid or “oligonucleotide” or grammatical equivalents herein refer to at least two nucleotides covalently linked together.
  • a nucleic acid of the present invention is preferably single-stranded or double stranded and will generally contain phosphodiester bonds, although in some cases, as outlined below, nucleic acid analogs are included that may have alternate backbones, comprising, for example, phosphoramide (Beaucage et al, Tetrahedron 49(10):1925, 1993) and references therein; Letsinger, J. Org. Chem. 35:3800, 1970; Sblul et al, Eur. J. Biochem.
  • nucleic acids include those with positive backbones (Denpcy et al, Proc. Natl. Acad. Sci. USA, 92:6097, 1995); non-ionic backbones (U.S. Pat. Nos. 5,386,023; 5,637,684; 5,602,240; 5,216,141 and 4,469,863; Angew, Chem. Intl. Ed. English 30:423, 1991; Letsinger et al, 1988 supra; Letsinger et al, Nucleoside & Nucleotide 13:1597, 1994; Chapters 2 and 3, ASC Symposium Series 580, Carbohydrate Modifications in Antisense Research , Ed.
  • test agent refers to an agent that is to be screened in one or more of the assays described herein.
  • the agent can be virtually any chemical compound. It can exist as a single isolated compound or can be a member of a chemical (e.g. combinatorial) library. In a particularly preferred embodiment, the test agent will be a small organic molecule.
  • agent may be replaced with “compound”, “molecule”, “medicament” and the like as listed above.
  • a “gene” includes a genomic gene or a cDNA molecule.
  • the terms “gene”, “cDNA”, “nucleic acid molecule” and “nucleotide sequence” may be used interchangeably.
  • a “nucleic acid molecule” may be RNA or DNA.
  • a “biomarker” may be the gene or gene product.
  • a “gene product” may be a protein or RNA.
  • one aspect of the present invention contemplates a method for the treatment or prophylaxis of a bone pathology of reducing the risk of development of a bone pathology in a subject, said method comprising administering to said subject an effective amount of an agent which modulates expression of genetic material or the activity of encoded products of the genetic material wherein the genetic material is differentially expressed in unfused versus fused calvarial sutures.
  • the present invention further provides a method for promoting bone growth or health in a subject, said method comprising administering to said subject an effective amount of an agent which modulates expression of genetic material or the activity of encoded products of the genetic material wherein the genetic material is differentially expressed in unfused versus fused calvarial sutures.
  • a particular embodiment of the present invention provides a method for the treatment or prophylaxis of a condition selected from one or more of bone cancer, a bone mineralization deficiency, fracture, a suture-based cranial abnormality, a cytoskeletal abnormality, osteoporosis or other biochemical or structural abnormality or condition, said method comprising administering to said subject an agent which modulates the level of expression of a gene or gene product which is up- or down-regulated in unfused sutures compared to fused sutures.
  • biomarkers for bone cancer include but are not limited to GPC3, RBP4, C1QTNF3, FMOD, WIF1, PRELP, PTN and CYFIP2 which have expression profiles shown in Table 5.
  • the present invention provides, therefore, a set of biomarkers comprising one or more genes or gene products differentially expressed in unfused sutures compared to fused sutures in a subject.
  • genes up-regulated in unfused sutures include but are not limited to MFAP4, RBP4, IL11RA, AMPH, INHBA, C1QTNF3, PRELP, FBLN1, ANGPTL2, AGC1, FMOD, OLFM1, C1orf24, AGC1, SSPN, PTN, MN1, TNN, EGFR, ADCY2, PDZRN3, SPON1, GPC3, HAPLN1, BCL11B, FLRT3, STXBP6, THBS2, KIAA0992, COL3A1, PAM, LSS, COL11A1, TOX, TRIM2, COL8A2, CRISPLD2, BHLHB3, EPHB2, DUSP10, COL11A1, OLFM1, TUBB2, SETBP1, ROR1, TGFB2, ISLR, PRSS11, COL16A1, S100A10, COL8A2, LOXL1, TRIM2, POSTN, LOXL2, CCND2, SSPN, ZCWCC2, ITGB
  • genes up-regulated in fused sutures include but are not limited to CYFIP2, ABCG1, ANAXA3, FABP4, DPYD, RNASE6, CHD7, HIST1H1E, CASP1, FLI1, ATF7IP2, ST6GAL1, MMD, LOC54103, PTPRE, PTPN22, TNFSF10, RAB11FIP1, MYCBP, RASSF2, SCAP2, HHEX, CD163, C18orf1, RAB27A, LOC54103, IL7R, GPR126, P2RY14, ARHGAP15, FCER1G, RGS2, HLA-DMB, PLSCR1, TRIM22, FAM60A, CD300A, BLM, PARP8, LAPTM5, CG018, LIG4, RAC2, RAB20, LOC93349, GENX-3414, E2 F5, DKFZP586A0522, ACSL1, OAS2, IQGAP2, CLEC2D, HLA-DMA
  • biomarkers include but are not limited to COL8A2, PRELP, RBP4, C1QTNF3, GPC3, CYFIP2, MFAP4, AMPH, IL11RA, INHBA, WIF1, ANXA3, CASP1, SHOX2 and PTN.
  • GPC3, RBP4 and C1QTNF3 are highly expressed in unfused sutures whereas WIF1 and CASP1 are highly expressed in fused and fusing sutures.
  • Reference to the above genes include polymorphic variants mutants and derivatives thereof as well as homologs thereof.
  • another aspect of the present invention contemplates a method of treating or reducing the risk of development of a bone pathology in a subject, said method comprising administering to said subject an agent which down-regulates a gene or gene product selected from the list comprising MFAP4, RBP4, IL11RA, AMPH, INHBA, C1QTNF3, PRELP, FBLN1, ANGPTL2, AGC1, FMOD, OLFM1, C1orf24, AGC1, SSPN, PTN, MN1, TNN, EGFR, ADCY2, PDZRN3, SPON1, GPC3, HAPLN1, BCL11B, FLRT3, STXBP6, THBS2, KIAA0992, COL3A1, PAM, LSS, COL11A1, TOX, TRIM2, COL8A2, CRISPLD2, BHLHB3, EPHB2, DUSP10, COL11A1, OLFM1, TUBB2, SETBP1, ROR1, TGFB2, ISLR, PRSS11,
  • the up-regulation of the above genes is at least 2-fold higher than controls and at least up to 100-fold such as 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99 or 100-fold up-regulation.
  • a value of from at least about 2-fold to at least about 40-fold up-regulation is preferred and a value of from at least about 10-fold to about 40-fold is particularly preferred.
  • the present invention also provides a genetic construct comprising an encoding nucleic acid molecule or an antisense version thereof or which otherwise targets a nucleic acid molecule selected from the list comprising a nucleic acid molecule whose expression is up-regulated or down-regulated in unfused versus fused sutures such as a gene selected from MFAP4, RBP4, IL11RA, AMPH, INHBA, C1QTNF3, PRELP, FBLN1, ANGPTL2, AGC1, FMOD, OLFM1, C1orf24, AGC1, SSPN, PTN, MN1, TNN, EGFR, ADCY2, PDZRN3, SPON1, GPC3, HAPLN1, BCL11B, FLRT3, STXBP6, THBS2, KIAA0992, COL3A1, PAM, LSS, COL11A1, TOX, TRIM2, COL8A2, CRISPLD2, BHLHB3, EPHB2, DUSP10, COL11A1, OLFM1, TUBB2,
  • Particularly useful target genes are COL8A2, PRELP, RBP4, C1QTNF3, CYFIP2, MFAP4, AMPH, IL11RA, INHBA, WIF1, ANXA3, CASP1, SHOX2 and PTN.
  • Therapeutic protocols encompass manipulation of gene expression, gene replacement and modulation of protein activity or protein replacement therapy.
  • Diagnostic protocols include genetic and protein based assays aimed at determining the level of gene expression or gene products and/or the presence of any mutations in the genes or gene products.
  • the present invention further provides, therefore, the use of one or more genes or gene products differentially expressed in unfused sutures compared to fused sutures in a subject in the manufacture of a medicament for the treatment of a bone pathology.
  • the differential expression is conveniently determined in patients with craniosynostosis.
  • the present invention contemplates targeting genes whose aberrant expression leads to premature fusion of sutures but which may also be associated with other bone pathologies as listed above.
  • the present invention provides a method of screening for an agent which modulates the level of activity of a target gene or target gene product associated with a bone pathology.
  • the method includes contacting a test cell containing a target gene with a test agent and detecting a change in the expression level of the target gene or the activity of target gene product in the test cell as compared to the expression of the target gene or the activity of the target gene product in a control cell where a difference in expression level of the target gene or the activity of the target gene product in the test cell and the control cell indicates that said agent may modulate the symptoms of a bone pathology.
  • the control is a negative control cell contacted with the test agent at a lower concentration than the test cell.
  • the expression level of the target gene is detected by measuring the level of the target gene mRNA in said cell and/or the level of target gene product is detected by determining the level of protein in the biological cell.
  • the present invention provides, therefore, therapeutic agents which interact with a target gene, target gene transcript or other gene product (such as a protein).
  • a target gene such as a protein
  • Alanine scans of proteins for example, are commonly used to define such protein motifs.
  • These parts or residues constituting the active region of the compound are known as its “pharmacophore”.
  • the terms “peptide”, “polypeptide” or “protein” may be used interchangeably.
  • the pharmacophore Once the pharmacophore has been found, its structure is modeled according to its physical properties, e.g. stereochemistry, bonding, size and/or charge, using data from a range of sources, e.g. spectroscopic techniques, x-ray diffraction data and NMR. Computational analysis, similarity mapping (which models the charge and/or volume of a pharmacophore, rather than the bonding between atoms) and other techniques can be used in this modeling process.
  • a range of sources e.g. spectroscopic techniques, x-ray diffraction data and NMR.
  • Computational analysis, similarity mapping which models the charge and/or volume of a pharmacophore, rather than the bonding between atoms
  • other techniques can be used in this modeling process.
  • Modeling can be used to generate agents which interact with the linear sequence or a three-dimensional configuration.
  • a template molecule is then selected onto which chemical groups which mimic the pharmacophore can be grafted.
  • the template molecule and the chemical groups grafted onto it can conveniently be selected so that the therapeutic agent is easy to synthesize, is likely to be pharmacologically acceptable, and does not degrade in vivo, while retaining the biological activity of the lead compound.
  • the agent is peptide-based
  • further stability can be achieved by cyclizing the peptide, increasing its rigidity.
  • the agents found by this approach can then be screened to see whether they have the target property, or to what extent they can modulate the activity of a target protein or modulation expression of a target gene. Further optimization or modification can then be carried out to arrive at one or more final agents for in vivo or clinical testing.
  • the goal of rational drug design is to produce structural analogs or antagonists of biologically active polypeptides of interest or of small molecules with which they interact (e.g. agonists, antagonists, inhibitors or enhancers) in order to fashion drugs which are, for example, more active or stable forms of the polypeptide, or which, for example, enhance or interfere with the function of a polypeptide in vivo (see, e.g. Hodgson, BioTechnology 9:19-21, 1991).
  • Agents are also contemplated by the present invention which regulate expression of target genes. This could involve, inter alia, providing gene function to a cell such as in gene therapy, or, it could involve inhibiting gene function using gene silencing constructs including antisense oligonucleotides or expression constructs.
  • a target nucleic acid sequence or a part of a nucleic acid sequence such as a nucleic acid sequence capable of regulating nucleic acid expression may be introduced into a cell in a vector such that the nucleic acid sequence remains extrachromosomal. In such a situation, the nucleic acid sequence will be expressed by the cell from the extrachromosomal location.
  • Vectors for introduction of nucleic acid sequence both for recombination and for extrachromosomal maintenance are known in the art and any suitable vector may be used.
  • Methods for introducing nucleic acids into cells such as electroporation, calcium phosphate co-precipitation and viral transduction are known in the art.
  • viruses have been used as nucleic acid transfer vectors or as the basis for preparing nucleic acid transfer vectors, including papovaviruses (e.g. SV40, Madzak et al, J Gen Virol 73:1533-1536, 1992), adenovirus (Berkner, Curr Top Microbiol Immunol 158:39-66, 1992; Berkner et al, BioTechniques 6:616-629, 1988; Gorziglia and Kapikian, J Virol 66:4407-4412, 1992; Quantin et al, Proc Natl Acad Sci USA 89:2581-2584, 1992; Rosenfeld et al, Cell 68:143-155, 1992; Wilkinson et al, Nucleic Acids Res 20:233-2239, 1992; Stratford-Perricaudet et al, Hum Gene Ther 1:241-256, 1990; Schneider et al, Nat Genetics 18:180-183, 1998), vac
  • Non-viral nucleic acid transfer methods are known in the art such as chemical techniques including calcium phosphate co-precipitation, mechanical techniques, for example, microinjection, membrane fusion-mediated transfer via liposomes and direct DNA uptake and receptor-mediated DNA transfer.
  • Viral-mediated nucleic acid transfer can be combined with direct in vivo nucleic acid transfer using liposome delivery, allowing one to direct the viral vectors to particular cells.
  • the retroviral vector producer cell line can be injected into particular tissue. Injection of producer cells would then provide a continuous source of vector particles.
  • the present invention further contemplates the introduction of antisense and sense molecules such as polynucleotide sequences, which are useful in silencing transcripts of target genes. Ribozymes, micro RNAs, synthetic RNAi, DNA-derived RNAi as well as double stranded RNAs may also be introduced. Both pre-transcriptional and post-transcriptional gene silencing is contemplated including antisense silencing.
  • polynucleotide vectors containing all or a portion of a gene locus encoding the expression product of a target gene may be placed under the control of a promoter in an antisense or sense orientation and introduced into a cell. Expression of such an antisense or sense construct within a cell interferes with target transcription and/or translation.
  • the engineered genetic molecules encode oligonucleotides and similar species for use in modulating the expression of target genes, i.e. the oligonucleotides induce pre-transcriptional or post-transcriptional gene silencing.
  • the constructs may encode inter alia micro RNA, dsRNA, hairpin RNAs, RNAi, siRNA or DNA.
  • target gene is used for convenience to encompass DNA encoding the target gene product, RNA (including pre-mRNA and mRNA or portions thereof) transcribed from such DNA, and also cDNA derived from such RNA.
  • the present invention provides a method for treatment or prophylaxis of diseases or conditions characterized by being or causing a bone pathology comprising administering to a subject an agent capable of regulating expression of a gene which is differentially expressed in un-fused sutures versus fused sutures.
  • This method includes promoting bone growth or overall health.
  • a non-genetic therapeutic agent may be administered.
  • the agents of the present invention can be combined with one or more pharmaceutically acceptable carriers and/or diluents to form a pharmacological composition.
  • Pharmaceutically acceptable carriers can contain a physiologically acceptable compound that acts to, e.g., stabilize, or increase or decrease the absorption or clearance rates of the pharmaceutical compositions of the invention.
  • Physiologically acceptable compounds can include, e.g., carbohydrates, such as glucose, sucrose, or dextrans, antioxidants, such as ascorbic acid or glutathione, chelating agents, low molecular weight proteins, compositions that reduce the clearance or hydrolysis of the peptides or polypeptides, or excipients or other stabilizers and/or buffers.
  • Detergents can also be used to stabilize or to increase or decrease the absorption of the pharmaceutical composition, including liposomal carriers.
  • physiologically acceptable compounds include wetting agents, emulsifying agents, dispersing agents or preservatives which are particularly useful for preventing the growth or action of microorganisms.
  • Various preservatives are well known and include, e.g., phenol and ascorbic acid.
  • a pharmaceutically acceptable carrier including a physiologically acceptable compound depends, for example, on the route of administration of the modulatory agent of the invention and on its particular physio-chemical characteristics.
  • Administration of the agent, in the form of a pharmaceutical composition may be performed by any convenient means known to one skilled in the art.
  • Routes of administration include, but are not limited to, respiratorally, intratracheally, nasopharyngeally, intravenously, intraperitoneally, subcutaneously, intracranially, intradermally, intramuscularly, intraoccularly, intrathecally, intracereberally, intranasally, orally, rectally, patch and implant.
  • the compounds can be formulated into solid or liquid preparations such as capsules, pills, tablets, lozenges, powders, suspensions or emulsions.
  • any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents, suspending agents, and the like in the case of oral liquid preparations (such as, for example, suspensions, elixirs and solutions); or carriers such as starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like in the case of oral solid preparations (such as, for example, powders, capsules and tablets).
  • tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed. If desired, tablets may be sugar-coated or enteric-coated by standard techniques.
  • the active agent can be encapsulated to make it stable to passage through the gastrointestinal tract while at the same time allowing for passage across the blood brain barrier, see, e.g, International Patent Publication Number WO 96/11698.
  • Agents of the present invention when administered orally, may be protected from digestion. This can be accomplished either by complexing the agent with a composition to render it resistant to acidic and enzymatic hydrolysis or by packaging the agent in an appropriately resistant carrier such as a liposome.
  • Means of protecting compounds from digestion are well known in the art, see, e.g. Fix, Pharm Res 13:1760-1764, 1996; Samanen et al, J Pharm Pharmacol 48:119-135, 1996; U.S. Pat. No. 5,391,377, describing lipid compositions for oral delivery of therapeutic agents.
  • the pharmaceutical forms suitable for injectable use include sterile aqueous solutions (where water-soluble) or dispersions and sterile powders for the preparation of sterile injectable solutions or dispersion or may be in the form of a cream or other form suitable for topical application. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi.
  • the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils.
  • the proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of superfactants.
  • the prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride.
  • Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminium monostearate and gelatin.
  • Sterile injectable solutions are prepared by incorporating the agents in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the various sterilised active ingredient into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above.
  • the preferred methods of preparation are vacuum drying and the freeze-drying technique which yield a powder of the active ingredient plus any additional desired ingredient from previously sterile-filtered solution thereof.
  • the agent may be dissolved in a pharmaceutical carrier and administered as either a solution or a suspension.
  • suitable carriers are water, saline, dextrose solutions, fructose solutions, ethanol, or oils of animal, vegetative or synthetic origin.
  • the carrier may also contain other ingredients, for example, preservatives, suspending agents, solubilizing agents, buffers and the like.
  • the agents When the agents are being administered intrathecally, they may also be dissolved in cerebrospinal fluid.
  • penetrants appropriate to the barrier to be permeated can be used for delivering the agent.
  • penetrants are generally known in the art e.g. for transmucosal administration, bile salts and fusidic acid derivatives.
  • detergents can be used to facilitate permeation.
  • Transmucosal administration can be through nasal sprays or using suppositories e.g. Sayani and Chien, Crit Rev Ther Drug Carrier Syst 13:85-184, 1996.
  • the agents are formulated into ointments, creams, salves, powders and gels.
  • Transdermal delivery systems can also include patches.
  • the agents of the invention can be delivered using any system known in the art, including dry powder aerosols, liquids delivery systems, air jet nebulizers, propellant systems, and the like, see, e.g., Patton, Nat Biotech 16:141-143, 1998; product and inhalation delivery systems for polypeptide macromolecules by, e.g., Dura Pharmaceuticals (San Diego, Calif.), Aradigm (Hayward, Calif.), Aerogen (Santa Clara, Calif.), Inhale Therapeutic Systems (San Carlos, Calif.), and the like.
  • the pharmaceutical formulation can be administered in the form of an aerosol or mist.
  • the formulation can be supplied in finely divided form along with a surfactant and propellant.
  • the device for delivering the formulation to respiratory tissue is an inhaler in which the formulation vaporizes.
  • Other liquid delivery systems include, for example, air jet nebulizers.
  • the agents of the subject invention can also be administered in sustained delivery or sustained release mechanisms, which can deliver the formulation internally.
  • sustained delivery or sustained release mechanisms which can deliver the formulation internally.
  • biodegradable microspheres or capsules or other biodegradable polymer configurations capable of sustained delivery of an agent can be included in the formulations of the instant invention (e.g. Putney and Burke, Nat Biotech 16:153-157, 1998).
  • compositions of the invention in vesicles composed of substances such as proteins, lipids (for example, liposomes), carbohydrates, or synthetic polymers.
  • pharmacokinetics see, e.g., Remington's.
  • the pharmaceutical formulations comprising agents of the present invention are incorporated in lipid monolayers or bilayers such as liposomes, see, e.g., U.S. Pat. Nos. 6,110,490; 6,096,716; 5,283,185 and 5,279,833.
  • the invention also provides formulations in which water-soluble modulatory agents of the invention have been attached to the surface of the monolayer or bilayer.
  • peptides can be attached to hydrazide-PEG-(distearoylphosphatidyl)ethanolamine-containing liposomes (e.g. Zalipsky et al, Bioconjug Chem 6:705-708, 1995).
  • Liposomes or any form of lipid membrane such as planar lipid membranes or the cell membrane of an intact cell e.g. a red blood cell, can be used.
  • Liposomal formulations can be by any means, including administration intravenously, transdermally (Vutla et al, J Pharm Sci 85:5-8, 1996), transmucosally, or orally.
  • the invention also provides pharmaceutical preparations in which the agents of the invention are incorporated within micelles and/or liposomes (Suntres and Shek, J Pharm Pharmacol 46:23-28, 1994; Woodle et al, Pharm Res 9:260-265, 1992).
  • Liposomes and liposomal formulations can be prepared according to standard methods and are also well known in the art see, e.g., Remington's; Akimaru et al, Cytokines Mol Ther 1:197-210, 1995; Alving et al, Immunol Rev 145:5-31, 1995; Szoka and Papahadjopoulos, Ann Rev Biophys Bioeng 9:467-508, 1980, U.S. Pat. Nos. 4,235,871, 4,501,728 and 4,837,028.
  • compositions of the invention can be administered in a variety of unit dosage forms depending upon the method of administration. Dosages for typical pharmaceutical compositions are well known to those of skill in the art. Such dosages are typically advisorial in nature and are adjusted depending on the particular therapeutic context, patient tolerance, etc. The amount of agent adequate to accomplish this is defined as the “effective amount”.
  • the dosage schedule and effective amounts for this use, i.e. the “dosing regimen” will depend upon a variety of factors, including the stage of the disease or condition, the severity of the disease or condition, the general state of the patient's health, the patient's physical status, age, pharmaceutical formulation and concentration of active agent, and the like. In calculating the dosage regimen for a patient, the mode of administration also is taken into consideration.
  • the dosage regimen must also take into consideration the pharmacokinetics, i.e. the pharmaceutical composition's rate of absorption, bioavailability, metabolism, clearance, and the like. See, e.g., Remington's; Egleton and Davis, Peptides 18:1431-1439, 1997; Langer, Science 249:1527-1533, 1990.
  • the agents and/or pharmaceutical compositions defined in accordance with the present invention may be co-administered with one or more other agents.
  • co-administered means simultaneous administration in the same formulation or in two different formulations via the same or different routes or sequential administration by the same or different routes.
  • simultaneous administration is meant a time difference of from seconds, minutes, hours or days between the administration of the two types of agents and/or pharmaceutical compositions. Co-administration of the agents and/or pharmaceutical compositions may occur in any order.
  • the present invention also facilitates the development of diagnostic and/or prognostic assays and reagents useful for identifying the presence of a disease or condition, or the propensity to develop a disease or condition, or the severity of a disease or condition wherein the disease or condition is characterized by being a bone pathology such as a cranial abnormality associated with fused sutures.
  • the present invention contemplates a method of diagnosing or predicting the development of a bone pathology in a subject, said method comprising isolating a sample from a potentially affected bone or bone tissue from the subject, said sample comprising genetic material or a protein or RNA encoded by the genetic material and determining the pattern of expression of the genetic material wherein up-regulation or down-regulation of expression of particular genetic material relative to a control is indicative of a bone pathology or risk of developing same.
  • the assays may, therefore, be genetic or protein based. Particularly useful diagnostic targets are listed above.
  • a single target may be identified as being up- or down-regulated or an array of two or more may provide a profile which in itself provides an indication of the presence of a bone pathology or a risk of development of same.
  • a particularly preferred diagnostic assay is nucleic acid based such as but not limited to detecting mutations in DNA and levels and mutations of mRNA.
  • Reference herein to DNA and mRNA means nucleic acid molecules associated with the biomarkers.
  • mutations in a biomarker or set of biomarkers are predictive of the potential for the development of a bone pathology such as but not limited to craniosynostosis.
  • Reference herein to a sample from which a nucleic acid or protein based assay is conducted includes a biological sample such as serum, whole blood, plasma, mucus, tissue fluid, tissue extract, bone tissue biopsy or other source of genes or proteins associated with a bone pathology.
  • Expression levels of a gene can be altered by changes in the transcription of the gene product (i.e. transcription of mRNA) and/or by changes in translation of the gene product (i.e. translation of the protein) and/or by post-translation modification(s) (e.g. protein folding, glycosylation, etc.). Expression levels may also be affected by mutation levels in the gene.
  • preferred assays of the present invention include assaying for level of transcribed mRNA, level of translated protein, activity or translated protein and/or mutations including polymorphisms in DNA or mRNA.
  • changes in expression level can be detected by measuring changes in mRNA and/or a nucleic acid derived from the mRNA (e.g. reverse-transcribed cDNA, etc.).
  • a nucleic acid sample for such analysis.
  • the nucleic acid is found in or derived from a biological sample.
  • biological sample refers to a sample obtained from an organism or from components (e.g. cells) of an organism. The sample may be of any biological tissue or fluid. Biological samples may also include organs or sections of tissues such as frozen sections taken for histological purposes. Generally, however, a bone sample may be taken or, in the case of craniosynostosis, the sample is from a calvarial suture.
  • control is generally the expression pattern of genes in unfused versus fused calvarial sutures.
  • the nucleic acid e.g. mRNA nucleic acid derived from mRNA
  • the nucleic acid is, in certain preferred embodiments, isolated from the sample according to any of a number of methods well know to those skilled in the art. Methods of isolating mRNA are well known to those of skill in the art. For example, methods of isolation and purification of nucleic acids are described in detail in Tijssen, Ed, Chapter 3 of Laboratory Techniques in Biochemistry and Molecular Biology Hybridization with Nucleic Acid Probes, Part I, Theory and Nucleic Acid Preparation , Elsevier, N.Y. and Tijssen, Ed.
  • the “total” nucleic acid is isolated from a given sample using, for example, an acid guanidinium-phenol-chloroform extraction method and polyA+mRNA is isolated by oligo dT column chromatography or by using (dT)n magnetic beads (see Sambrook et al, Molecular Cloning: A Laboratory Manual (2 nd ed.) 1-3:1989 or Ausubel et al, Current Protocols in Molecular Biology, F , Greene Publishing and Wiley-Interscience, New York, 1987).
  • PCR polymerase chain reaction
  • LCR ligase chain reaction
  • detecting and/or quantifying the target gene transcript(s) can be routinely accomplished using nucleic acid hybridization techniques (see, Sambrook et al, 1989 supra).
  • one method for evaluating the presence, absence, or quantity of target gene reverse-transcribed cDNA involves a “Southern Blot”.
  • the DNA e.g. reverse-transcribed target mRNA
  • a probe specific for the target gene is hybridized to a probe specific for the target gene.
  • Comparison of the intensity of the hybridization signal from the target gene probe with a “control” probe e.g. a probe for a “housekeeping gene” provides an estimate of the relative expression level of the target nucleic acid.
  • the target gene mRNA can be directly quantified in a Northern blot.
  • the mRNA is isolated from a given cell sample using, for example, an acid guanidinium-phenol-chloroform extraction method. The mRNA is then electrophoresed to separate the RNA species and the mRNA is transferred from the gel to a nitrocellulose membrane.
  • labeled probes are used to identify and/or quantify the target gene mRNA. Appropriate controls (e.g. probes to housekeeping genes) provide a reference for evaluating relative expression level.
  • in situ hybridization An alternative means for determining the target gene expression level is in situ hybridization.
  • In situ hybridization assays are well known (e.g. Angerer, Meth. Enzymol 152:649, 1987).
  • in situ hybridization comprises the following major steps: (1) fixation of tissue or biological structure to be analyzed; (2) prehybridization treatment of the biological structure to increase accessibility of target DNA or RNA, and to reduce non-specific binding; (3) hybridization of the mixture of nucleic acids to the nucleic acid in the biological structure or tissue; (4) post-hybridization washes to remove nucleic acid fragments not bound in the hybridization; and (5) detection of the hybridized nucleic acid fragments.
  • the reagent used in each of these steps and the conditions of use vary depending on the particular application.
  • amplification-based assays can be used to measure target gene expression (transcription) level.
  • the target nucleic acid sequences act as template(s) in amplification reaction(s) (e.g. Polymerase Chain Reaction (PCR) or reverse-transcription PCR(RT-PCR)).
  • amplification reaction e.g. Polymerase Chain Reaction (PCR) or reverse-transcription PCR(RT-PCR)
  • PCR Polymerase Chain Reaction
  • RT-PCR reverse-transcription PCR
  • Arrays are a multiplicity of different “probe” or “target” nucleic acids (or other compounds) attached to one or more surfaces (e.g. solid, membrane or gel).
  • the multiplicity of nucleic acids (or other moieties) is attached to a single contiguous surface or to a multiplicity of surfaces juxtaposed to each other.
  • Arrays particularly nucleic acid arrays can be produced according to a wide variety of methods well known to those of skill in the art.
  • “low density” arrays can simply be produced by spotting (e.g. by hand using a pipette) different nucleic acids at different locations on a solid support (e.g. a glass surface, a membrane, etc.).
  • Arrays can also be produced using oligonucleotide synthesis technology.
  • U.S. Pat. No. 5,143,854 and PCT Patent Publication Nos. WO 90/15070 and 92/10092 teach the use of light-directed combinatorial synthesis of high density oligonucleotide arrays. Synthesis of high density arrays is also described in U.S. Pat. Nos. 5,744,305; 5,800,992 and 5,445,934.
  • alterations in expression of a target gene can be detected and/or quantified by detecting and/or quantifying the amount and/or activity of a translated target gene encoded polypeptide.
  • the polypeptide(s) encoded by a target gene can be detected and quantified by any of a number of methods well known to those of skill in the art. These may include analytic biochemical methods such as electrophoresis, capillary electrophoresis, high performance liquid chromatography (HPLC), thin layer chromatography (TLC), hyperdiffusion chromatography, and the like, or various immunological methods such as fluid or gel precipitin reactions, immunodiffusion (single or double), immunoelectrophoresis, radioimmunoassay (RIA), enzyme-linked immunosorbent assays (ELISAs), immunofluorescent assays, Western blotting, and the like.
  • analytic biochemical methods such as electrophoresis, capillary electrophoresis, high performance liquid chromatography (HPLC), thin layer chromatography (TLC), hyperdiffusion chromatography, and the like
  • various immunological methods such as fluid or gel precipitin reactions, immunodiffusion (single or double), immunoelectroph
  • the target gene expression product e.g. proteins
  • an electrophoretic protein separation e.g. a 1- or 2-dimensional electrophoresis.
  • Means of detecting proteins using electrophoretic techniques are well known to those of skill in the art (see Scope, Protein Purification , Springer-Verlag, NY, 1982; Duetscher, Methods in Enzymology Vol. 182: Guide to Protein Purification , Academic Press, Inc. NY, 1990).
  • Western blot (immunoblot) analysis is used to detect and quantify the presence of polypeptide(s) of the subject invention in the sample.
  • This technique generally comprises separating sample proteins by gel electrophoresis on the basis of molecular weight, transferring the separated proteins to a suitable solid support (such as a nitrocellulose filter, a nylon filter, or derivatized nylon filter), and incubating the sample with the antibodies that specifically bind the target polypeptide(s).
  • the present invention extends to antibodies to target polypeptides.
  • Polyclonal antibodies may conveniently be used, however, the use of monoclonal antibodies in an immunoassay or for capture is particularly preferred because of the ability to produce them in large quantities and the homogeneity of the product.
  • the preparation of hybridoma cell lines for monoclonal antibody production is derived by fusing an immortal cell line and lymphocytes sensitized against the immunogenic preparation (i.e. comprising 35-LM polypeptide) or can be done by techniques which are well known to those who are skilled in the art. (See, for example, Douillard and Hoffman, Basic Facts about Hybridomas, in Compendium of Immunology Vol. II, ed.
  • Single chain antibodies or transgenic mice expressing humanized antibodies or other recognition proteins may also be used.
  • Useful proteins in this regard include diabodies, peptide mimetics and antibody fragments such as scFv fragments and Fab fragments.
  • the present invention further provides therefore the application of biochemical techniques to render an antibody derived from one animal or avian creature substantially non-immunogenic in another animal or avian creature of the same or different species.
  • the biochemical process is referred to herein as “de-immunization”.
  • Reference herein to “de-immunization” includes processes such as complementary determinant region (CDR) grafting, “reshaping” with respect to a framework region of an immuno-interactive molecule and variable (v) region mutation, all aimed at reducing the immunogenicity of an immuno-interactive molecule in a particular host (eg. a human subject).
  • the preferred antibody is a monoclonal antibody, derived from one animal or avian creature and which exhibits reduced immunogenicity in another animal or avian creature from the same or different species such as but not limited to humans if used in a human form therapeutic or imaging purposes.
  • the present invention extends to antibodies or their antigen binding fragments.
  • Antibodies may be polyclonal or monoclonal.
  • Polyclonal antibodies to a target polypeptide can be prepared using methods well-known to those of skill in the art (see, for example, Green et al, Immunochemical Protocols (Manson ed):1-5, 1992; Williams et al, DNA Cloning 2: Expression Systems, 2 nd Ed., Oxford University Press 1995). Although polyclonal antibodies are typically raised in animals such as rats, mice, rabbits, goats, or sheep, a target polypeptide antibody of the present invention may also be derived from a subhuman primate antibody. General techniques for raising diagnostically and therapeutically useful antibodies in baboons may be found, for example, in Goldenberg et al, International Patent Publication No. WO 91/11465, 1991 and in Losman et al, Int. J. Cancer 46:310, 1990.
  • variable region domain may be of any size or amino acid composition and will generally comprise at least one hypervariable amino acid sequence responsible for antigen binding embedded in a framework sequence.
  • variable (V) region domain may be any suitable arrangement of immunoglobulin heavy (V H ) and/or light (V L ) chain variable domains.
  • V H immunoglobulin heavy
  • V L light chain variable domains.
  • the V region domain may be monomeric and be a V H or V L domain where these are capable of independently binding antigen with acceptable affinity.
  • V region domain may be dimeric and contain V H -V H , V H -V L , or V L -V L , dimers in which the V H and V L chains are non-covalently associated (abbreviated hereinafter as F v ).
  • the chains may be covalently coupled either directly, for example via a disulphide bond between the two variable domains, or through a linker, for example a peptide linker, to form a single chain domain (abbreviated herein after as scF v ).
  • variable region domain may be any naturally occurring variable domain or an engineered version thereof.
  • engineered version is meant a variable region domain that has been created using recombinant DNA engineering techniques.
  • engineered versions include those created for example from natural antibody variable regions by insertions, deletions or changes in or to the amino acid sequences of the natural antibodies.
  • Particular examples of this type include those engineered variable region domains containing at least one CDR and optionally one or more framework amino acids from antibody and the remainder of the variable region domain from a second antibody.
  • variable region domain may be covalently attached at a C-terminal amino acid to at least one other antibody domain or a fragment thereof.
  • a V H domain is present in the variable region domain this may be linked to an immunoglobulin C H 1 domain or a fragment thereof.
  • a V L domain may be linked to a C K domain or a fragment thereof.
  • the antibody may be a Fab fragment wherein the antigen binding domain contains associated V H and V L domains covalently linked at their C-termini to a C H 1 and C K domain respectively.
  • the C H 1 domain may be extended with further amino acids, for example to provide a hinge region domain as found in a Fab fragment, or to provide further domains, such as antibody CH2 and CH3 domains.
  • CDR peptides (“minimal recognition units”) can be obtained by constructing genes encoding the CDR of an antibody of interest. Such genes are prepared, for example, by using the polymerase chain reaction to synthesize the variable region from RNA or antibody-producing cells (see, for example, Larrick et al, Methods: A Companion to Methods in Enzymology 2:106, 1991; Courtneay-Luck, Monoclonal Antibodies: Production, Engineering and Clinical Application , Ritter et al (eds), Cambridge University Press:166, 1995 and Ward et al, Monoclonal Antibodies: Principles and Applications Birch et al, Wiley-Liss, Inc.:137, 1995.
  • Antibodies for use in the subject invention are preferably monoclonal (prepared by conventional immunization and cell fusion procedures) or in the case of fragments, derived therefrom using any suitable standard chemical such as reduction or enzymatic cleavage and/or digestion techniques, for example by treatment with pepsin. More specifically, monoclonal anti-TGF-beta binding-protein antibodies can be generated utilizing a variety of techniques.
  • Rodent monoclonal antibodies to specific antigens may be obtained by methods known to those skilled in the art (see, for example, Kohler et al, 1975 supra and Coligan et al, Current Protocols in Immunology 1, John Wiley & Sons 1991; Picksley et al, DNA Cloning 2: Expression Systems, 2 nd Edition , Glover et al (eds), page 93 Oxford University Press, 1995).
  • monoclonal antibodies can be obtained by injecting mice with a composition comprising a target gene product, verifying the presence of antibody production by removing a serum sample, removing the spleen to obtain B-lymphocytes, fusing the B-lymphocytes with myeloma cells to produce hybridomas, cloning the hybridomas, selecting positive clones which produce antibodies to the antigen, culturing the clones that produce antibodies to the antigen, and isolating the antibodies from the hybridoma cultures.
  • an anti-target polypeptide antibody of the present invention may be derived from a human monoclonal antibody.
  • Human monoclonal antibodies are obtained from transgenic mice that have been engineered to produce specific human antibodies in response to antigenic challenge.
  • elements of the human heavy and light chain locus are introduced into strains of mice derived from embryonic stem cell lines that contain targeted disruptions of the endogenous heavy chain and light chain loci.
  • the transgenic mice can synthesize human antibodies specific for human antigens and the mice can be used to produce human antibody-secreting hybridomas. Methods for obtaining human antibodies from transgenic mice are described, for example, by Green et al, Nature Genet. 7:1994, Lonberg et al, Nature 368:856, 1994 and Taylor et al, Int. Immun. 6:579, 1994).
  • Monoclonal antibodies can be isolated and purified from hybridoma cultures by a variety of well-established techniques. Such isolation techniques include affinity chromatography with Protein-A Sepharose, size-exclusion chromatography and ion-exchange chromatography (see for example, Baines et al, Methods in Molecular Biology 10:79-104, 1992).
  • antibody fragments can be obtained by pepsin or papain digestion of whole antibodies by conventional methods.
  • antibody fragments can be produced by enzymatic cleavage of antibodies with pepsin to provide a 5 S fragment denoted F(ab′) 2 .
  • This fragment can be further cleaved using a thiol reducing agent to produce 3.5 S Fab′ monovalent fragments.
  • the cleavage reaction can be performed using a blocking group for the sulfhydryl groups that result from cleavage of disulfide linkages.
  • cleaving antibodies such as separation of heavy chains to form monovalent light-heavy chain fragments, further cleavage of fragments, or other enzymatic, chemical or genetic techniques may also be used, so long as the fragments bind to the antigen that is recognized by the intact antibody.
  • the antibody may be a recombinant or engineered antibody obtained by the use of recombinant DNA techniques involving the manipulation and re-expression of DNA encoding antibody variable and/or constant regions.
  • DNA is known and/or is readily available from DNA libraries including for example phage-antibody libraries (see Chiswell and McCafferty, J. Tibtech 10:80-84, 1992) or where desired can be synthesized. Standard molecular biology and/or chemistry procedures may be used to sequence and manipulate the DNA, for example, to introduce codons to create cysteine residues, to modify, add or delete other amino acids or domains as desired.
  • One or more replicable expression vectors containing the DNA encoding a variable and/or constant region may be prepared and used to transform an appropriate cell line, e.g. a non-producing myeloma cell line, such as bacterial (e.g. E. coli ) in which production of the antibody will occur.
  • an appropriate cell line e.g. a non-producing myeloma cell line, such as bacterial (e.g. E. coli ) in which production of the antibody will occur.
  • the DNA sequence in each vector should include appropriate regulatory sequences, particularly a promoter and leader sequence operably linked to a variable domain sequence. Particular methods for producing antibodies in this way are generally well known and routinely used.
  • the antibody according to the present invention may have one or more effector or reporter molecules attached to it and the subject invention extends to such modified proteins.
  • a reporter molecule may be a detectable moiety or label such as an enzyme, or other reporter molecule, including a dye, radionuclide, luminescent group, fluorescent group, or biotin, or the like.
  • the target polypeptide specific immunoglobulin or fragment thereof may be radiolabeled for diagnostic or therapeutic applications. Techniques for radiolabeling of antibodies are known in the art, see Adams, In Vivo 12:11-21, 1998; Hiltunen, Acta Oncol. 32:931-939, 1993.
  • the effector or receptor molecules may be attached to the antibody through any available amino acid side-chain, terminal acid, or where present, carbohydrate functional group located in the antibody, provided that the attachment or the attachment process does not adversely affect the binding properties and the usefulness of the molecule.
  • Particular functional groups include, for example, any free amino, imino, thiol, hydroxyl, carboxyl or aldehyde group. Attachment of the antibody and the effector and/or reporter molecule(s) may be achieved via such groups and an appropriate functional group in the effector or reporter molecules.
  • the linkage may be direct or indirect through spacing or bridging groups.
  • the antibodies of the present invention may be used both therapeutically to inhibit or target a protein or may be used diagnostically to screen for levels of target proteins.
  • the gene product or antibodies or nucleic acid molecules described above may be labeled with a variety of compounds, including for example, fluorescent molecules, toxins and radionuclides.
  • fluorescent molecules include fluorescin, Phycobili proteins such as phycoerythrin, rhodamine, Texas red and luciferase.
  • toxins include ricin, abrin, diphtheria toxin, cholera toxin, gelonin, pokeweed antiviral protein, tritin, Shigella toxin, and Pseudomonas exotosin A.
  • radionuclides include Cu-64, Ga-67, GA-68, Zr-89, Ru-97, Tc-99m, Rh-105, Pd-109, In-111, I-123, I-125, I-131, Re-186, Re-188, Au-198, Au-199, Pb-203, At-211, Pb-212 and Bi-212.
  • the antibodies described above may also be labeled or conjugated to one partner of a ligand binding pair.
  • Representative examples include avidin-biotin, streptavidin-biotin, and riboflavin-riboflavin binding protein.
  • kits and compositions also form part of the present invention.
  • Such kits may comprise diagnostic or therapeutic agents, singularly or in combination with other agents.
  • another aspect of the present invention is directed to the use of an agent which up-regulates or down-regulates a gene listed in Table 2 or 3 or 4 in the manufacture of a medicament or diagnostic agent for a bone pathology in a subject.
  • FIG. 2 provides mRNA and protein validation of differential expression identified by microanalysis. The expression patterns of RBP4 and GPC3 are shown in FIG. 3 .
  • RBP4 is a binder and carrier of retinol (vitamin A). All trans-retinoic acid (RA) is a metabolite of retinol and is a known craniosynostosis causing teratogen (Gardner et al, Int. J. Epidemiol 27(1):64-67, 1998; Yip et al, Teratology 21(1):29-38, 1980). Studies show RA increases differentiation of osteoblasts, decreases proliferation and induces bone nodule formation in vitro (Song et al, J. Cell Physiol. 202(1):255-262, 2005; Cowan et al, Tissue Eng. 11(3-4):645-658, 2005).
  • RBP4 in suture mesenchyme may be to sequester retinol. Once its expression is downregulated (during the fusing stage) retinol is released and converted to RA, which then stimulates osteoblast differentiation and bone formation.
  • An inhibitor of RBP4 may, therefore, promote osteogenesis, while delivery of the secreted protein will maintain proliferation of early stage osteoblasts and limit terminal differentiation.
  • C1QTNF3 was initially identified in a chondrocyte cell line after treatment with TGF-[3]. Embryonic expression analysis in mice show a high level of expression in prechondrocytic mesenchymal cells, but it is undetectable in mature chondrocytes (Maeda et al, J. Biol. Chem. 276(5):3628-3634, 2001). Our work is the first to identify C1QTNF3 in calvarial suture preosteoblastic mesenchyme and suggests a possible function in regulating mesenchymal condensations during skeletal development.
  • GPC3 is a cell surface heparan sulphate proteoglycan. Loss of GPC3 causes Simpson-Golabi Behmel syndrome, which is characterised by pre- and post-natal overgrowth, cleft palate, short broad nose, prognathism, widened nasal bridge and disproportionably large head. Double mutant mice for BMP4 and GPC3 have increased phenotype, suggesting GPC3 is involved in BMP signaling. Ectopic GPC3 expression decreases BMP4 expression and blocks BMP7 activity (Midorikawa et al, Int. J. Cancer 103(4):455-465, 2003; Paine-Saunders et al, Dev. Biol.
  • GPC3 acts to limit BMP induced osteoblast differentiation.
  • GPC3 deficient mice also present with polydactyl, a common phenotype seen in patients with craniosynostosis syndromes.
  • GPC3 has also been shown to bind FGF2 and overexpression of GPC3 suppressed FGF2-induced cell proliferation in hepatocytes (Midorikawa et al, 2003 supra). This suggests that GPC3 also interacts in FGF signaling on osteoprogenitors, as FGFR mutations are the common cause of multiple craniosynostosis syndromes.
  • GPC3 has been shown to suppress non-canonical Wnt signaling and activate canonical Wnt/ ⁇ -Catenin signaling and in doing so regulates cell proliferation (Song et al, J. Biol. Chem. 280(3):2116-2125, 2005; De Cat et al, J. Cell Biol. 163(3):625-635, 2003).
  • GPC3 may control cell growth within osteogenic mesenchyme, but inhibition leads to increased growth, while inducing GPC3 suppresses signaling pathways involving FGFs, BMPs and non-canonical Wnts.
  • MFAP4 is a putative ECM protein involved in cell adhesion or cell to cell interaction. Deletion of MFAP4 causes Smith-Magenis syndrome, clinical features of which are brachycephaly, midface hypoplasia, prognathism and growth retardation (Zhao et al, Hum. Mol. Genet. 4(4):589-597, 1995). The skull malformation suggests MFAP4 may be vial component of suture mesenchyme. Bovine Mfap4 has been identified as a collagen binder and may aid in ECM organization (Lausen et al, Biol. Chem. 274(45):32234-32240, 1999).
  • FMOD is a small leucine-rich proteoglycan (SLRP) and is involved in ECM assembly. It competes for binding with TGF ⁇ 1, 2 and 3 and may sequester it in the ECM (Hildebrand, 1994). It is a regulator for collagen fibrillogenesis, and its RNA expression is upregulated just before the onset of mineralization. It bind collagen, retarding the rate of fibril formation leading to thinner fibrils. It is been identified as being upregulated by BMP2 dependent differentiation of C2C12 premyoblasts into the osteogenic lineage. It may regulate cellular growth or migration.
  • SLRP small leucine-rich proteoglycan
  • OGN is a small leucine-rich keratan sulphate proteoglycan which induces ectopic bone formation in conjunction with transforming growth factor beta. It is thought that osteoglycin may regulate cellular growth as its transcription is up regulated by growth factors and tumor suppressor protein p53. Furthermore, it has been shown to inhibit multinucleated cell formation and subsequently limit osteoclast formation and activity. Mice deficient in OGN also have increased collagen fibril diameter, indicating a role in collagen fibrillogenesis.
  • PRELP is a heparin-binding small leucine-rich proteoglycan (SLRP) in connective tissue extracellular matrix.
  • SLRP small leucine-rich proteoglycan
  • PRELP binds the basement membrane heparan sulfate proteoglycan perlecan.
  • PRELP binds collagen type I and type II. It is that PRELP functions as a molecule anchoring basement membranes to the underlying connective tissue.
  • WIF1 is an antagonist of Wnt signaling and has recently been shown to have strong expression in late phase differentiation of C2C12 and MC3T3E-1 preosteoblast cell lines. Continuous activation of Wnt signaling reduces osteoblast differentiation, thus WIF1 may be required for controlling osteoblast maturation (Vaes et al, Bone 36(5):803-811, 2005).
  • ANXA3 is a member of the calcium-dependent phospholipid-binding protein family. Limited information is known about ANXA3, however, general AnxA expression has been identified to be significantly increased during progression of osteoarthritis. S100A proteins have been shown to interact with AnxA5 and AnxA6 and as a number of S100A proteins are also upregulated with ANXA3, they may interact with ANXA3 as well. Retinol can bind AnxA6 and inhibition of ion channel activity of AnxAs has been shown to reverse the apoptotic effects of RA (Balcerzak et al, FEBS Lett. 580:3065-3069, 2006). RA has also been shown to stimulate cell differentiation and expression of AnxAs in avian growth plate chondrocytes, suggesting a link between ANXA3 and retinoic acid induced osteogenesis.
  • CASP1 has been shown to induce cell apoptosis and may function in various developmental stages. This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing.
  • SHOX2 is a member of the homeo box family and has a C-terminal 14-amino acid residue motif characteristic for craniofacially expressed homeodomain proteins.
  • Limited embryo expression analysis identified SHOX2 in condensing CART1 laginous mesenchyme in the nose and palate In the fore limb bud, transcripts were restricted to undifferentiated mesenchyme condensing around the developing bone (Rudiger et al, Proc. Natl. Acad. Sci. USA 95(5):2406-2411, 1998).
  • CYFIP2 cytoplasmic FMR1 (fragile X mental retardation 1) interacting protein, is an actin regulatory protein and a mediator of p53-dependent apoptosis. It increases fibronectin-mediated binding in Jurkat and CD4(+) cells (Mayne et al, Eur J. Immunol. 34:1217-27, 2004). These studies suggest that overabundance of CYFIP2 protein facilitates increased adhesion properties of T cells from MS patients. CYFIP2 may therefore be involved in an immune-like response during suture fusion.
  • biomarkers are shown in Table 4.
  • FIG. 1 shows the level of expression of one particular biomarker, RBP4 in fused and unfused sutures.
  • Table 5 shows the expression of several preferred biomarkers in human bone cancer cell lines.
  • One set of preferred biomarkers, GPC3, RBP4 and C1QTNF3, is more highly expressed in unfused sutures whereas another set of preferred biomarkers, ANXA3, WIF1 and CASP1, is more highly expressed in fused and fusing sutures.
  • the human osteosarcoma cell lines are SaOS (American Type Culture Collection [ATCC] HTB-85), SJSA-1 (ATCC CRL-2098), U-2 OS (HTB-96), MG-63 (ATCC CR1-1427), HOS (ATCC CRL-1543) and G-292 (ATCC CRL-1423).

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